A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171339



Internal ID21501348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:990758..990758hg38UCSC Ensembl
chrY:901493..901493hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614384
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171339
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer